Human Phenotype Ontology 
Grandparent Node:
expand
Abnormality of the pancreas (HP:0001732)help
Parent Node:
expand
Abnormal pancreas morphology (HP:0012090)help
..Starting node
..expand
Pancreatic cysts (HP:0001737)help
Term ID: 1737
Name: Pancreatic cysts
Synonym: Multiple pancreatic cysts; Pancreatic cyst; Pancreatic cysts
Definition: A cyst of the pancreas that possess a lining of mucous epithelium.
Comments:
Reference: HP:0001737
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandAbnormal pancreas size (HP:0012094) help
..expandAbnormal pancreatic duct morphology (HP:0030992) help
..expandAnnular pancreas (HP:0001734) help
..expandEctopic pancreatic tissue (HP:0006278) help
..expandHyperechogenic pancreas (HP:0006276) help
..expandPancreas divisum (HP:0030994) help
..expandPancreatic abscess (HP:0025079) help
..expandPancreatic calcification (HP:0005213) help
..expandPancreatic dysplasia (HP:0005232) help
..expandPancreatic fibrosis (HP:0100732) help
..expandPancreatic fistula (HP:0100844) help
..expandPancreatic lymphangiectasis (HP:0006273) help
..expandPancreatic pseudocyst (HP:0005206) help
InputHPO IDHPO termDistanceGeneGene id entrezHGNC IDDiseaseIdDiseaseNameFrequencyOnsetHGMD variantsClinVar variants
 
HPO disease - gene - phenotype typical associations:
 
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0001737HP:0001737Pancreatic cysts0ALG5 CL E G H2988020266ORPHA:730Autosomal dominant polycystic kidney diseaseHP:0040283 - Occasional
HP:0001737HP:0001737Pancreatic cysts0ALG9 CL E G H7979615672ORPHA:730Autosomal dominant polycystic kidney diseaseHP:0040283 - Occasional93
HP:0001737HP:0001737Pancreatic cysts0B9D1 CL E G H2707724123ORPHA:564Meckel syndromeHP:0040283 - Occasional28
HP:0001737HP:0001737Pancreatic cysts0B9D2 CL E G H8077628636ORPHA:564Meckel syndromeHP:0040283 - Occasional34
HP:0001737HP:0001737Pancreatic cysts0BICC1 CL E G H8011419351ORPHA:730Autosomal dominant polycystic kidney diseaseHP:0040283 - Occasional5
HP:0001737HP:0001737Pancreatic cysts0CC2D2A CL E G H5754529253ORPHA:564Meckel syndromeHP:0040283 - Occasional247
HP:0001737HP:0001737Pancreatic cysts0CCND1 CL E G H5951582ORPHA:892Von Hippel-Lindau diseaseHP:0040283 - Occasional1
HP:0001737HP:0001737Pancreatic cysts0CCND1 CL E G H5951582OMIM:193300Von hippel-lindau syndrome.1
HP:0001737HP:0001737Pancreatic cysts0CEP290 CL E G H8018429021ORPHA:564Meckel syndromeHP:0040283 - Occasional342
HP:0001737HP:0001737Pancreatic cysts0CSPP1 CL E G H7984826193ORPHA:564Meckel syndromeHP:0040283 - Occasional57
HP:0001737HP:0001737Pancreatic cysts0DNAJB11 CL E G H5172614889ORPHA:730Autosomal dominant polycystic kidney diseaseHP:0040283 - Occasional
HP:0001737HP:0001737Pancreatic cysts0DZIP1L CL E G H19922126551ORPHA:731Autosomal recessive polycystic kidney diseaseHP:0040284 - Very rare4
HP:0001737HP:0001737Pancreatic cysts0GANAB CL E G H231934138ORPHA:730Autosomal dominant polycystic kidney diseaseHP:0040283 - Occasional6
HP:0001737HP:0001737Pancreatic cysts0GLIS3 CL E G H16979228510OMIM:610199Diabetes mellitus, neonatal, with congenital hypothyroidismHP:0040283 - Occasional143
HP:0001737HP:0001737Pancreatic cysts0IFT140 CL E G H974229077ORPHA:730Autosomal dominant polycystic kidney diseaseHP:0040283 - Occasional148
HP:0001737HP:0001737Pancreatic cysts0IFT140 CL E G H974229077OMIM:266920Short-rib thoracic dysplasia 9 with or without polydactyly148
HP:0001737HP:0001737Pancreatic cysts0MKS1 CL E G H549037121ORPHA:564Meckel syndromeHP:0040283 - Occasional127
HP:0001737HP:0001737Pancreatic cysts0NPHP3 CL E G H270317907OMIM:267010MECKEL SYNDROME, TYPE 7; MKS7157
HP:0001737HP:0001737Pancreatic cysts0NPHP3 CL E G H270317907OMIM:208540Renal-Hepatic-Pancreatic dysplasia.157
HP:0001737HP:0001737Pancreatic cysts0OFD1 CL E G H84812567OMIM:311200Orofaciodigital syndrome I201
HP:0001737HP:0001737Pancreatic cysts0OFD1 CL E G H84812567ORPHA:2750Orofaciodigital syndrome type 1HP:0040283 - Occasional201
HP:0001737HP:0001737Pancreatic cysts0PKD1 CL E G H53109008ORPHA:730Autosomal dominant polycystic kidney diseaseHP:0040283 - Occasional342
HP:0001737HP:0001737Pancreatic cysts0PKD2 CL E G H53119009ORPHA:730Autosomal dominant polycystic kidney diseaseHP:0040283 - Occasional106
HP:0001737HP:0001737Pancreatic cysts0PKHD1 CL E G H53149016ORPHA:731Autosomal recessive polycystic kidney diseaseHP:0040284 - Very rare563
HP:0001737HP:0001737Pancreatic cysts0PKHD1 CL E G H53149016OMIM:263200Polycystic kidney disease 4 with or without polycystic liver disease.563
HP:0001737HP:0001737Pancreatic cysts0RBM8A CL E G H99399905OMIM:274000Thrombocytopenia-absent radius syndrome.10
HP:0001737HP:0001737Pancreatic cysts0RPGRIP1 CL E G H5709613436ORPHA:564Meckel syndromeHP:0040283 - Occasional109
HP:0001737HP:0001737Pancreatic cysts0RPGRIP1L CL E G H2332229168ORPHA:564Meckel syndromeHP:0040283 - Occasional167
HP:0001737HP:0001737Pancreatic cysts0TCTN1 CL E G H7960026113ORPHA:564Meckel syndromeHP:0040283 - Occasional45
HP:0001737HP:0001737Pancreatic cysts0TCTN2 CL E G H7986725774ORPHA:564Meckel syndromeHP:0040283 - Occasional76
HP:0001737HP:0001737Pancreatic cysts0TCTN3 CL E G H2612324519ORPHA:564Meckel syndromeHP:0040283 - Occasional31
HP:0001737HP:0001737Pancreatic cysts0TMEM107 CL E G H8431428128ORPHA:564Meckel syndromeHP:0040283 - Occasional4
HP:0001737HP:0001737Pancreatic cysts0TMEM216 CL E G H5125925018ORPHA:564Meckel syndromeHP:0040283 - Occasional45
HP:0001737HP:0001737Pancreatic cysts0TMEM231 CL E G H7958337234ORPHA:564Meckel syndromeHP:0040283 - Occasional33
HP:0001737HP:0001737Pancreatic cysts0TMEM237 CL E G H6506214432ORPHA:564Meckel syndromeHP:0040283 - Occasional82
HP:0001737HP:0001737Pancreatic cysts0TMEM67 CL E G H9114728396ORPHA:564Meckel syndromeHP:0040283 - Occasional166
HP:0001737HP:0001737Pancreatic cysts0TXNDC15 CL E G H7977020652ORPHA:564Meckel syndromeHP:0040283 - Occasional2
HP:0001737HP:0001737Pancreatic cysts0VHL CL E G H742812687ORPHA:892Von Hippel-Lindau diseaseHP:0040283 - Occasional490
HP:0001737HP:0001737Pancreatic cysts0VHL CL E G H742812687OMIM:193300Von hippel-lindau syndrome.490
HP:0001737HP:0001737Pancreatic cysts0WDR19 CL E G H5772818340OMIM:614377Nephronophthisis 13HP:0040283 - Occasional95
HP:0001737HP:0001737Pancreatic cysts0WDR19 CL E G H5772818340OMIM:616307Senior-Loken syndrome 8.95
HP:0001737HP:0001737Pancreatic cysts0XPNPEP3 CL E G H6392928052OMIM:613159Nephronophthisis-Like nephropathy 1HP:0040283 - Occasional109


Genes (35) :ALG5 ALG9 B9D1 B9D2 BICC1 CC2D2A CCND1 CEP290 CSPP1 DNAJB11 DZIP1L GANAB GLIS3 IFT140 MKS1 NPHP3 OFD1 PKD1 PKD2 PKHD1 RBM8A RPGRIP1 RPGRIP1L TCTN1 TCTN2 TCTN3 TMEM107 TMEM216 TMEM231 TMEM237 TMEM67 TXNDC15 VHL WDR19 XPNPEP3

Diseases (16) :ORPHA:730 ORPHA:564 ORPHA:892 OMIM:193300 ORPHA:731 OMIM:610199 OMIM:266920 OMIM:267010 OMIM:208540 OMIM:311200 ORPHA:2750 OMIM:263200 OMIM:274000 OMIM:614377 OMIM:616307 OMIM:613159
 

Human Phenotype Ontology(HPO) is developed by the Human Phenotype Ontology Consortium. The version used here is December 15 2022 release.